ZMP
itga10
Ensembl ID:
ZFIN ID:
Human Orthologue:
ITGA10
Human Description:
integrin, alpha 10 [Source:HGNC Symbol;Acc:6135]
Mouse Orthologue:
Itga10
Mouse Description:
integrin, alpha 10 Gene [Source:MGI Symbol;Acc:MGI:2153482]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36072 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22786 | Essential Splice Site | Available for shipment | Available now |
sa11418 | Essential Splice Site | Available for shipment | Available now |
sa45567 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15068 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36072
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011224 | Nonsense | 411 | 1170 | 11 | 30 |
ENSDART00000139859 | Nonsense | 411 | 1174 | 12 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 16068017)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14412909 |
GRCz11 | 16 | 14303029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGGGAGGCATCCTGAAAGAAAGCAAAGAAGGGCAGCTTATGCCCCCA[C/T]GAGAGGCCTTTGAGAAAGAGTTCCCACTGGAGCTCAAGAATCATGCAGCC
Long Flanking Sequence:
GATAACTTTAGACTTTAGATTTGATGCATTGTCAAAAATGTAGTACCTTTCTGTGCTGACAATAAACAATTAATAACTCTTACCAAAACATTTAGAATAGTAGAGCACACAAATGTTTATTGCTGTACTTAGCATTAGCATTGATTTGATTACAGCACTTTACACTCTACATAACGATATTTTATTTTAAAGAATGCAATGTGTTTTCTTGTTACAGGCACTTTAGGATACAATGAAAGTGCCTTTCTTATGGAGATGTCTCAGATTGGGTTTTCAACACACATTTTGGATGTGAGTTTCAGTGTAATCTATGTCTATGTGAAGTTGTGCCTAAATTCAAATGTTTGAATCGATATACTGAGATATATGCAGATGCTTCAGAACATGTATTCATGCTGTGAACTTCACTGCAGGATGGCATCTTGTTTGGCATGGTGGGAGCCTACGATTGGGAGGGAGGCATCCTGAAAGAAAGCAAAGAAGGGCAGCTTATGCCCCCA[C/T]GAGAGGCCTTTGAGAAAGAGTTCCCACTGGAGCTCAAGAATCATGCAGCCTACCTAGGTAATGTCTAAATATGCAGTTTTTAATCTTCAATGATTCCTTGATATTTCGAATAGATTTGTGACATCACACTAAATGCACATTTTTAAGGAGAATAACTTACTTTAGCATAGTTTTTCAGATAAACCAGCCTGTTCACTTAGCATGTGTCTTACATATCTGCAAACATAGGATTTTTATGTTTTAGTACAGTCAAAAACTTACATACAACCCATTTAAATTCACTAACAGAAGAACAAGTTTAAGAACAAACTCATTTACATACTCATGTGATGAATTAAGGGTAAAGTTTATATGAGAAGTTCAAATGTGCTTATAAATACTATAAATTATGCAATTATTCATGAAGGAGACCAAATGTTTACATTTTTTAAATATATTTGGTATGTTATTTTATTAACATTATAGATAAAACTCAAGAAACTATGAACAAAATAATAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22786
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011224 | Essential Splice Site | 595 | 1170 | 14 | 30 |
ENSDART00000139859 | Essential Splice Site | 595 | 1174 | 15 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 16064754)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14409646 |
GRCz11 | 16 | 14299766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACATCTACCATGGCGATGAATACTACATCATACCTCAGTATAAACAAG[T/G]AAATATAGCACCGTTTCATGGTTACAGACAGATCAATGGGTTAGTTCAAT
Long Flanking Sequence:
AGATTGCTCAATATTTTTCCCCTTTCTGTCCAGATCGGCTCATATTTTGGCAGCGAGGTATGCGTGGTGGACGTGGATCAGGATGGAATAACAGATATCCTGCTTATAGCTGCTCCAATGTTTCTGGGAGCCGGAAACAAAGAAACAGGCAAAGTCTACGTCTTCTGTCTGGATGGGGTGAGAGATTCAATGTTCTGTATTTTGACTAAAACCTTGCAGCTGGAAACATTTGATCTTCTAAAAGCTATTAGATGTTTAATCTACTTCCGAATATTTCTCTCTCTCTCTCTACTAGGATGGTTTTGCTCCCAACGGGACGCTGCATTCTCAGCAGAAGGCACAGGATGCACGCTTTGGTTATGCCATGGCTGTGGCCCCTGACCTCAACCATGATGGATACACTGATCTGCTCGTGGGAGCTCCGCTTGAGGATGACCACCAGGGAGCTCTTTACATCTACCATGGCGATGAATACTACATCATACCTCAGTATAAACAAG[T/G]AAATATAGCACCGTTTCATGGTTACAGACAGATCAATGGGTTAGTTCAATCATAGTCCCCATTTAGGGCTCTGCAATTAATCAAAATTCATTCCCATCATAACAGAAAGTGATCTTTTAAGTTAGCTGCATGCCTAAATGGTCGAATACCTTCAGAAATGGGTCAAAACAATGGCACCTAGCGATTATGCACACAAATTATTATTAATATTTTCACACTTGTTTGTTATATAATAAATAAACATGAATAGTTAAGAATGAAAATTCATGTGTAACAGTAAATCGGATCTGTGTTATATTGATATTCCTCCTGCTGATAGTTTTGAGGATTTTTTCTCTCTCTTTGTTTGCTTTTAGTTGTTCATTCTGCTGTGCCCAAGTAAACACATTCTGCATTTATGGGTAAACTATCCCATTTAGTGTCATATTTCTTTTGAATAATGTATTCTTGCCAATCAAATATATACATTTAAAAAACAAAGTAGTGTTGAATTGTAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11418
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011224 | Essential Splice Site | 742 | 1170 | 17 | 30 |
ENSDART00000139859 | Essential Splice Site | 746 | 1174 | 18 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 16058355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14403247 |
GRCz11 | 16 | 14293367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTTCGTGTTGGAGAGACCAAGTGCTACATCTTGCCATTTCACGTTTTT[G/A]TAAGTCTTCAGAAAATCAATGAAGCAATGGAAATGTACATTTAGTCGGTC
Long Flanking Sequence:
AAGTACTGTATTTATTTATCTTGGTTCAAAATACAGCTGTTCATTGCTAGTTCATGTTAACTCACAGTGCAATAACTAAGCACAACTTTGTATTCTAATGTTGCATCAGTAAATGTTGAACTATGATTTAATCTATATTTAACTATATTTGAACTATAGTTTATGTTAGTAAAAATACAATTGCTTGAAACATTATTGTAGAGTGTGATTATTATGGTGTTAAATATACAAAATATATTACTGAGTGGTATTCTAGTAGGTGTATTCTTTAAATCATGGTAAAAGTGTTTGTTATTCAGTCTTTTTTTTTTTGCTGAAAAACTAAACAAAAAAAATTGTTTCATTTTTGACCCATAGATATGCAGGTGGGGGCCATGCTGGATGACAGAAAGATCTCAGCTCGTGCTTTGTTTGACTCCAACTCTCAGCGTCAGACCTTAATGAGCATCAGTGTTCGTGTTGGAGAGACCAAGTGCTACATCTTGCCATTTCACGTTTTT[G/A]TAAGTCTTCAGAAAATCAATGAAGCAATGGAAATGTACATTTAGTCGGTCAATACTGCAAAAAATGAGGCTGTATTGTTATAATGGTTTACTTACTGTACATTATACTTGCTAGTATATACTCATTGTTTTCAACCAAAAGTGTTCTTCTGCCAGTTTCTGACTTCCTTTATGCATCTAGGATACAGCCGATTACATCCGACCGATCAGCTTCACTTTACGCTTCAAAATCAATGACACAGAAAGCGGCCCGGTACTTGACGAGGGCTGGCCAACAACACACAAGAAGTCTGTGAGTGATTTTCAACTGCATTATTCATGCCTCAAAAACAGGAATATGAATGGATATTAGAAAAATATATAGGAATAGACTCATTTTACAAGAAACCTAGAGTTAAGCAATTGAGTTCTTACATTTTGAATACGTTCAGCTGATCTCCAAGTTTGGTGAGAGCATGTTTAGCTTAGCTTAGCATAAATCATTGAATCATATTAGATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45567
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011224 | Essential Splice Site | 886 | 1170 | 21 | 30 |
ENSDART00000139859 | Essential Splice Site | 890 | 1174 | 22 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 16055598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14400490 |
GRCz11 | 16 | 14290610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTCACTCGTGTAATGTCAGCTATCCTGTGTTTCGCTCTCAGTCAAAG[G/A]TAAGCTTCTGACAGTCAGATTCATCCAAACACTTACTAAGGTGTTTCAAT
Long Flanking Sequence:
TGAGTACTATTGCTGAATGATTAAGCATAAAAATAACAATAGCAACATAAAATAACTATTGTTTTTGTCTTTTGTGATTGCAAACAAGTGTTATTCCACTAAATATTGCTTTCTTGATATTTCTGCTATTGTATTATAAGTATCTATTTTTTTGTATTGTAATGTCCAAAAATGAATATAAACATTTTTTCATTATCATTGCCATTTTCTGAGGGAAAAAATAACTCTAAATGATAATATACTTTATTTCAATTTTGGAATAGATGTTATAAAACCATTACATATTACAGAATAAAACAAATCTTAACAATTAACTTAAATATATAAATCGAGATAAAAAAAACTCATGTAAATAAACCAAACTTTCTGCTTATTATTTTTCTCTTTTTCTCTCTGTCTTTCTGCAGGAAGATGCCCAGTTTAAGATTGAATGCACGGCTCTAGGCTCAAACAGTCACTCGTGTAATGTCAGCTATCCTGTGTTTCGCTCTCAGTCAAAG[G/A]TAAGCTTCTGACAGTCAGATTCATCCAAACACTTACTAAGGTGTTTCAATCCATTGATTAGAGATTTTCCAAATCGTCCCGTTTTCTCAGGTGAACTTCATGCTGGAATTTGAGTTCAGCTGTACGTCTCTCATCAGTAAAGTCCAGATGAGGCTCATTGCTTCCAGGTAAACACACACATCTTAAACCAATAACAAATTGACGAAGCACTGAGGTGGTCTTAACTCATTCAGAGGACCAGAATCAATCTTCCACTTTAATATTTTCACACAGTCATGTTTTTTTTTGTACTTAATTTATTCCAGACAACATTAGCCCCTTTCACACAGTGATACCGGTAAATATCTGGAAAATTTCCGGAACGACTTTACCGGTAAATTCAAAAAAGCGCTGTTCACACAGGCGAGGACGTTACAGAATTTTTCCGGAATACACACTACTCCTGAATACTTTTTTACTTTTTACCACTTTTTACTTTTGAGTAGTGTGTAGAACAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15068
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011224 | Essential Splice Site | 1114 | 1170 | 28 | 30 |
ENSDART00000139859 | Essential Splice Site | 1118 | 1174 | 29 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 16050687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 14395579 |
GRCz11 | 16 | 14285699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGAGAGTCCAATCTGATTACAWTGGGAAATGCTGCCCTCTTGAGGGAG[G/A]TGAGAGAACTGRRACTTTAAATTAGATGACTGGTACCGGTCAAAGATRAA
Long Flanking Sequence:
GAGCTAACCATAGAAAAGAGCAGGAAAACAATGGATGATTATGTTTCTCTTCTAGCATTCTAGCTGTGACTTCAACGTTTGGAAAAAATAAATTCAATCATCTCACTCAACGAAACTCAAAGGTCCAAGTCAGTAAGATAATTCGAACTTCCCATCGCTAAAAAACACTCAAAAAGGTTCATTTTGATTTCCAGAACTGCAGTTCGTCATGGTGTGTGGAGGTGATGTGTCACATCCAGCAGCTGCTCAAGGGACAGACAGCCTTGATTCGCATCACTAGGAGGATACATGACAGCTTCTTCAGACAGGTCAGCTAATCTCTCACATGCAGAGACAGACAGACTTGAGTGGGATGTGTTTGTGTTTCAGTTTCTAACCTCGTAATTACTATGTGCTCCTGTCAGGCCAAGTTCAAAGCAGTGACAATCGTAGGCTCCTACCAGCTTTCTGCTCGAGAGTCCAATCTGATTACAATGGGAAATGCTGCCCTCTTGAGGGAG[G/A]TGAGAGAACTGAGACTTTAAATTAGATGACTGGTACCGGTCAAAGATGAAAATTGAAAACAGAATATGAAAACTGCAACACTTTTTTACTTTATTATTATTATTATTAATTGGACAATAGAATGTGTCTTAAGTGTGTAATTTTTTTAAGAAAAAAAAAAAAAACACTAAATCACTCCCTGAGAGTATTCAATGAATATTGTTTAGTATATTATCATTATTCATTCATTAATTTTCCTTTGGCTTACTTCCTTATTAATATTATTATTATTATCATTATTATACATAGAAAATGTGGCAAATTTAGGGCCAATCTCATTTGATCACGGTAAAACTATTTAGATCATAGTACAGGCCAAAAATACACTAATTCAGTGTCATTTTTAATATTTATGGTACGTTTTACATAGTTGTTTTAACCATTTAATATGTAATACAATTTGTATAATAAAACATGATTATTTTATACATACATGTAAGAAATATGTTCTTTATTTTCAT
Associated Phenotype:
Not determined